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Results: 1-25 | 26-50 | 51-56
Results: 1-25/56
UGT1A PROMOTER POLYMORPHISM DIFFERENTLY CONTRIBUTES TO JAUNDICE IN INHERITED HEMOLYTIC-ANEMIAS OF NEWBORN
Authors: IOLASCON A FAIENZA MF GIORDANI L PERROTTA S MELONI MF GUGGIU G DELGIUDICE EM
Citation: A. Iolascon et al., UGT1A PROMOTER POLYMORPHISM DIFFERENTLY CONTRIBUTES TO JAUNDICE IN INHERITED HEMOLYTIC-ANEMIAS OF NEWBORN, European journal of human genetics, 6, 1998, pp. 4085-4085
REFINEMENT OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II LOCUS ON CHROMOSOME-20
Authors: TOTARO A CARELLA M GRIFA A VALENTINO MA GASPARINI P ZELANTE L DELGIUDICE EM DELAUNAY J PERROTTA S IOLASCON A
Citation: A. Totaro et al., REFINEMENT OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II LOCUS ON CHROMOSOME-20, European journal of human genetics, 6, 1998, pp. 4128-4128
DECISION-MAKING AT THE BEDSIDE - DIAGNOSIS OF HEREDITARY SPHEROCYTOSIS IN A TRANSFUSED INFANT
Authors: DELGIUDICE EM PERROTTA S LOMBARDI C IOLASCON A
Citation: Em. Delgiudice et al., DECISION-MAKING AT THE BEDSIDE - DIAGNOSIS OF HEREDITARY SPHEROCYTOSIS IN A TRANSFUSED INFANT, Haematologica, 83(4), 1998, pp. 347-349
HEREDITARY SPHEROCYTOSIS - FROM CLINICAL TO MOLECULAR DEFECTS
Authors: IOLASCON A DELGIUDICE EM PERROTTA S ALLOISIO N MORLE L DELAUNAY J
Citation: A. Iolascon et al., HEREDITARY SPHEROCYTOSIS - FROM CLINICAL TO MOLECULAR DEFECTS, Haematologica, 83(3), 1998, pp. 240-257
ON THE VALIDITY OF THE MAXIMUM PRINCIPLE AND OF THE EULER-LAGRANGE EQUATION FOR A MINIMUM PROBLEM DEPENDING ON THE GRADIENT
Authors: CELLINA A PERROTTA S
Citation: A. Cellina et S. Perrotta, ON THE VALIDITY OF THE MAXIMUM PRINCIPLE AND OF THE EULER-LAGRANGE EQUATION FOR A MINIMUM PROBLEM DEPENDING ON THE GRADIENT, SIAM journal on control and optimization (Print), 36(6), 1998, pp. 1987-1998
DECREASED BAND-3 ANION TRANSPORT ACTIVITY AND BAND-3 CLUSTERIZATION IN CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II
Authors: DEFRANCESCHI L TURRINI F DELGIUDICE EM PERROTTA S OLIVIERI O CORROCHER R MANNU F IOLASCON A
Citation: L. Defranceschi et al., DECREASED BAND-3 ANION TRANSPORT ACTIVITY AND BAND-3 CLUSTERIZATION IN CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II, Experimental hematology, 26(9), 1998, pp. 869-873
EXISTENCE OF SOLUTIONS FOR A CLASS OF NON CONVEX MINIMUM PROBLEMS
Authors: CELADA P PERROTTA S TREU G
Citation: P. Celada et al., EXISTENCE OF SOLUTIONS FOR A CLASS OF NON CONVEX MINIMUM PROBLEMS, Mathematische Zeitschrift, 228(1), 1998, pp. 177-199
HIGH-FREQUENCY OF DE-NOVO MUTATIONS IN ANKYRIN GENE (ANK1) IN CHILDREN WITH HEREDITARY SPHEROCYTOSIS
Authors: DELGIUDICE EM FRANCESE M NOBILI B MORLE L CUTILLO S DELAUNAY J PERROTTA S
Citation: Em. Delgiudice et al., HIGH-FREQUENCY OF DE-NOVO MUTATIONS IN ANKYRIN GENE (ANK1) IN CHILDREN WITH HEREDITARY SPHEROCYTOSIS, The Journal of pediatrics, 132(1), 1998, pp. 117-120
CHROMOSOMAL LOCALIZATION OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II (CDA-II)
Authors: IOLASCON A DELGIUDICE EM PERROTTA S NOBILI B ZELANTE L GRANATIERO M MELCHIONDA S DELAUNAY J GASPARINI P
Citation: A. Iolascon et al., CHROMOSOMAL LOCALIZATION OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II (CDA-II), British Journal of Haematology, 102(1), 1998, pp. 3-3
DYSKERATOSIS-CONGENITA - A CASE WITH EARLY-ONSET
Authors: NOBILI B MATARESE SMR DELGIUDICE EM PERROTTA S DURZO G
Citation: B. Nobili et al., DYSKERATOSIS-CONGENITA - A CASE WITH EARLY-ONSET, British Journal of Haematology, 102(1), 1998, pp. 44-45
CLINICAL AND MOLECULAR EVALUATION OF NONDOMINANT HEREDITARY SPHEROCYTOSIS (HS)
Authors: DELGIUDICE EM NOBILI B DURZO G ILARDO R FRANCESE M CONTE ML EBER SW IOLASCON A PERROTTA S
Citation: Em. Delgiudice et al., CLINICAL AND MOLECULAR EVALUATION OF NONDOMINANT HEREDITARY SPHEROCYTOSIS (HS), British Journal of Haematology, 102(1), 1998, pp. 302-302
FREQUENT DE-NOVO MONOALLELIC EXPRESSION OF BETA-SPECTRIN GENE (SPTB) IN CHILDREN WITH HEREDITARY SPHEROCYTOSIS AND ISOLATED SPECTRIN DEFICIENCY
Authors: DELGIUDICE EM LOMBARDI C FRANCESE M NOBILI B CONTE ML AMENDOLA G CUTILLO S IOLASCON A PERROTTA S
Citation: Em. Delgiudice et al., FREQUENT DE-NOVO MONOALLELIC EXPRESSION OF BETA-SPECTRIN GENE (SPTB) IN CHILDREN WITH HEREDITARY SPHEROCYTOSIS AND ISOLATED SPECTRIN DEFICIENCY, British Journal of Haematology, 101(2), 1998, pp. 251-254
GENETIC-HETEROGENEITY OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II
Authors: IOLASCON A DEMATTIA D PERROTTA S CARELLA M GASPARINI P DELILIERS GL
Citation: A. Iolascon et al., GENETIC-HETEROGENEITY OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II, Blood, 92(7), 1998, pp. 2593-2594
UGT1 PROMOTER POLYMORPHISM ACCOUNTS FOR INCREASED NEONATAL APPEARANCEOF HEREDITARY SPHEROCYTOSIS
Authors: IOLASCON A FAIENZA MF MORETTI A PERROTTA S DELGIUDICE EM
Citation: A. Iolascon et al., UGT1 PROMOTER POLYMORPHISM ACCOUNTS FOR INCREASED NEONATAL APPEARANCEOF HEREDITARY SPHEROCYTOSIS, Blood, 91(3), 1998, pp. 1093-1093
GENOMEWIDE SEARCH FOR DEHYDRATED HEREDITARY STOMATOCYTOSIS (HEREDITARY XEROCYTOSIS) - MAPPING OF LOCUS TO CHROMOSOME-16 (16Q23-QTER)
Authors: CARELLA M STEWART G AJETUNMOBI JF PERROTTA S GROOTENBOER S TCHERNIA G DELAUNAY J TOTARO A ZELANTE L GASPARINI P IOLASCON A
Citation: M. Carella et al., GENOMEWIDE SEARCH FOR DEHYDRATED HEREDITARY STOMATOCYTOSIS (HEREDITARY XEROCYTOSIS) - MAPPING OF LOCUS TO CHROMOSOME-16 (16Q23-QTER), American journal of human genetics, 63(3), 1998, pp. 810-816
INCREASED MEMBRANE-PROTEIN PHOSPHORYLATION AND ANION TRANSPORT ACTIVITY IN CHOREA-ACANTHOCYTOSIS
Authors: OLIVIERI O DEFRANCESCHI L BORDIN L MANFREDI M DELGIUDICE EM PERROTTA S DEVIVO M GUARINI P CORROCHER R
Citation: O. Olivieri et al., INCREASED MEMBRANE-PROTEIN PHOSPHORYLATION AND ANION TRANSPORT ACTIVITY IN CHOREA-ACANTHOCYTOSIS, Haematologica, 82(6), 1997, pp. 648-653
APPARENTLY NORMAL ANKYRIN CONTENT IN UNSPLENECTOMIZED HEREDITARY SPHEROCYTOSIS PATIENTS WITH THE INACTIVATION OF ONE ANKYRIN (ANK1) ALLELE
Authors: DELGIUDICE EM FRANCESE M POLITO R NOBILI B IOLASCON A PERROTTA S
Citation: Em. Delgiudice et al., APPARENTLY NORMAL ANKYRIN CONTENT IN UNSPLENECTOMIZED HEREDITARY SPHEROCYTOSIS PATIENTS WITH THE INACTIVATION OF ONE ANKYRIN (ANK1) ALLELE, Haematologica, 82(3), 1997, pp. 332-333
MEMBRANE CATION AND ANION TRANSPORT ACTIVITIES IN ERYTHROCYTES OF HEREDITARY SPHEROCYTOSIS - EFFECTS OF DIFFERENT MEMBRANE-PROTEIN DEFECTS
Authors: DEFRANCESCHI L OLIVIERI O DELGIUDICE EM PERROTTA S SABATO V CORROCHER R IOLASCON A
Citation: L. Defranceschi et al., MEMBRANE CATION AND ANION TRANSPORT ACTIVITIES IN ERYTHROCYTES OF HEREDITARY SPHEROCYTOSIS - EFFECTS OF DIFFERENT MEMBRANE-PROTEIN DEFECTS, American journal of hematology, 55(3), 1997, pp. 121-128
FUNCTIONAL OUTCOME AFTER LAPAROSCOPIC POSTERIOR RECTOPEXY FOR RECTAL PROLAPSE
Authors: ESPOSITO P CERBONE D VERDE S RUSSO F PERROTTA S CERBONE G
Citation: P. Esposito et al., FUNCTIONAL OUTCOME AFTER LAPAROSCOPIC POSTERIOR RECTOPEXY FOR RECTAL PROLAPSE, Gastrointestinal endoscopy, 45(4), 1997, pp. 646-646
FREQUENT DE-NOVO MUTATIONS OF THE ANK1 GENE MIMIC A RECESSIVE MODE OFTRANSMISSION IN HEREDITARY SPHEROCYTOSIS - 3 NEW ANK1 VARIANTS - ANKYRINS-BARI, NAPOLI-II AND ANZIO
Authors: RANDON J DELGIUDICE EM BOZON M PERROTTA S DEVIVO M IOLASCON A DELAUNAY J MORLE L
Citation: J. Randon et al., FREQUENT DE-NOVO MUTATIONS OF THE ANK1 GENE MIMIC A RECESSIVE MODE OFTRANSMISSION IN HEREDITARY SPHEROCYTOSIS - 3 NEW ANK1 VARIANTS - ANKYRINS-BARI, NAPOLI-II AND ANZIO, British Journal of Haematology, 96(3), 1997, pp. 500-506
NOVEL BAND-3 VARIANTS (BANDS 3-FOGGIA, NAPOLI-I AND NAPOLI-II) ASSOCIATED WITH HEREDITARY SPHEROCYTOSIS AND BAND-3 DEFICIENCY - STATUS OF THE D38A POLYMORPHISM WITHIN THE EPB3 LOCUS
Authors: DELGIUDICE EM VALLIER A MAILLET P PERROTTA S CUTILLO S IOLASCON A TANNER MJA DELAUNAY J ALLOISIO N
Citation: Em. Delgiudice et al., NOVEL BAND-3 VARIANTS (BANDS 3-FOGGIA, NAPOLI-I AND NAPOLI-II) ASSOCIATED WITH HEREDITARY SPHEROCYTOSIS AND BAND-3 DEFICIENCY - STATUS OF THE D38A POLYMORPHISM WITHIN THE EPB3 LOCUS, British Journal of Haematology, 96(1), 1997, pp. 70-76
PHLEBOTOMY TO REDUCE IRON OVERLOAD IN PATIENTS CURED OF THALASSEMIA BY BONE-MARROW TRANSPLANTATION
Authors: ANGELUCCI E MURETTO P LUCARELLI G RIPALTI M BARONCIANI D ERER B GALIMBERTI M GIARDINI C GAZIEV D POLCHI P ROVELLI A MONGUZZI W MASERA G PIGA A GAROFALO F GABUTTI V DIGREGORIO F ROMEO MA CAMMELLA A RUSSO G GALLISAI D BURRAI C COSTI C MARINARO AM ERBEIA M MAZZANI D NOBILI B PERROTTA S",FERRARA,"CUTILLO S MULAS G CAREDDU F MANCINI E ARGIOLU F ADDARI C RUGGIERO L DENUNZIO A TERZOLI S DASCOLA G BRUCIATELLI M SATTA AM BORGNAPIGNATTI C MARRADI P PUGGIONI G MURGIA T PORTA E POGGI V PINTABOCCALATTE MF POLIZZI B MARONI P CHELAZZI G ROCCO S ROTOLI B MANGIAGLI G BELLOMO G MINELLI P LAMANTIA A COLAROSSI M MARTINELLI L FERNANDO V TOMMASI G DEROSA C BUFARDI S MELCHIORRI G CARUSO V
Citation: E. Angelucci et al., PHLEBOTOMY TO REDUCE IRON OVERLOAD IN PATIENTS CURED OF THALASSEMIA BY BONE-MARROW TRANSPLANTATION, Blood, 90(3), 1997, pp. 994-998
HEREDITARY SPHEROCYTOSIS PATIENT WITH PROTEIN-4.2 NIPPON - THE FIRST CASE IN A NON-JAPANESE POPULATION
Authors: PERROTTA S POLITO R DEVIVO M NOBILI B CONTE ML IOLASCON A CUTILLO S DELGIUDICE EM
Citation: S. Perrotta et al., HEREDITARY SPHEROCYTOSIS PATIENT WITH PROTEIN-4.2 NIPPON - THE FIRST CASE IN A NON-JAPANESE POPULATION, Blood, 90(10), 1997, pp. 2714-2714
SHORT-TERM CYCLOSPORINE-A THERAPY FOR CHRONIC THROMBOCYTOPENIC PURPURA (ITP) IN CHILDHOOD
Authors: AMENDOLA G POGGI V PERROTTA S SPIEZA M DELVECCHIO L MATARESE SMR MIRAGLIA E DELGIUDICE EM NOBILI B
Citation: G. Amendola et al., SHORT-TERM CYCLOSPORINE-A THERAPY FOR CHRONIC THROMBOCYTOPENIC PURPURA (ITP) IN CHILDHOOD, Blood, 90(10), 1997, pp. 3069-3069
HEREDITARY SPHEROCYTOSIS DUE TO AN ELONGATED BAND-3 - BAND-3 VESUVIO
Authors: PERROTTA S NIGRO V POLITO R NOBILI B AMENDOLA G DEVIVO M CONTE ML CUTILLO S DELGIUDICE EM
Citation: S. Perrotta et al., HEREDITARY SPHEROCYTOSIS DUE TO AN ELONGATED BAND-3 - BAND-3 VESUVIO, Blood, 90(10), 1997, pp. 1186-1186
Risultati: 1-25 | 26-50 | 51-56